Evidence map›Paper›PMID 40528577›Full record

ArticleEpilepsia2025

GABRA2-related encephalopathy: Identification of two phenotypes with distinctive electroclinical features.

Marie Adamo-Croux, Chloé Angelini, Jérôme Aupy, Laurent Villard, Nathalie Villeneuve, Arnaud Chefdor, Yorsa Halleb, Maxime Colmard, Manon Degoutin, Gaetan Lesca and 6 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Epilepsia, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Marie Adamo-CrouxDepartment of Pediatric Neurology, Reference Center for Rare Epilepsies, CHU Bordeaux, Bordeaux, France.
Chloé AngeliniService de Génétique Médicale, CHU Bordeaux, Bordeaux, France.
Jérôme AupyDepartment of Clinical Neurosciences, Reference Center for Rare Epilepsies, CHU de Bordeaux, Bordeaux, France.ORCID https://orcid.org/0000-0001-7268-7479
Laurent VillardMarseille Medical Genetics (MMG), Aix Marseille University, INSERM, Marseille, France.
Nathalie VilleneuveDepartment of Pediatric Neurology, Assistance Publique - Hôpitaux de Marseille (AP-HM), La Timone Children's Hospital, Marseille, France.
Arnaud ChefdorDepartment of Pediatrics, Le Mans Hospital, Le Mans, France.
Yorsa HallebDepartment of Medical Genetics, Le Mans Hospital, Le Mans, France.
Maxime ColmardDépartement de Neuropédiatrie, CHU de Montpellier, Montpellier, France.
Manon DegoutinService de Génétique Médicale, CHU Bordeaux, Bordeaux, France.ORCID https://orcid.org/0009-0007-8398-834X
Gaetan LescaDepartment of Medical Genetics, member of European Reference Network EpiCARE, University Hospitals of Lyon (HCL), Lyon, France.ORCID https://orcid.org/0000-0001-7691-9492
Perrine CharlesDépartement de Génétique, Hôpital Pitié-Salpêtrière, Assistance Publique - Hôpitaux de Paris (AP-HP), Sorbonne Université, Paris, France.
Boris KerenDépartement de Génétique, Hôpital Pitié-Salpêtrière, Assistance Publique - Hôpitaux de Paris (AP-HP), Sorbonne Université, Paris, France.
Nicole ChemalyDepartment of Pediatric Neurology, Reference Center for Rare Epilepsies, Necker Enfants Malades University Hospital, Assistance Publique - Hôpitaux de Paris (AP-HP), Université Paris Cité, Paris, France.
Cyril GoizetService de Génétique Médicale, CHU Bordeaux, Bordeaux, France.
Mathieu MilhMarseille Medical Genetics (MMG), Aix Marseille University, INSERM, Marseille, France.ORCID https://orcid.org/0000-0002-2454-8543
Claire BarDepartment of Pediatric Neurology, Reference Center for Rare Epilepsies, CHU Bordeaux, Bordeaux, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathogenic variants in γ-aminobutyric acid type A (GABA

Indexed as

developmental and epileptic encephalopathyEEG biomarkerelectroclinical phenotypesGABAGABAA receptorGABRA2

Identifiers

PMID40528577
PMCPMC12371673

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.